ClinVar Miner

List of variants in gene MT-TH reported as benign for Juvenile myopathy, encephalopathy, lactic acidosis AND stroke

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
HGVS dbSNP
NC_012920.1(MT-CYB):m.12141A>G rs1603223565
NC_012920.1(MT-CYB):m.12142A>G rs1603223566
NC_012920.1(MT-CYB):m.12151A>G rs1603223576
NC_012920.1(MT-CYB):m.12161T>C rs386829147
NC_012920.1(MT-CYB):m.12166T>C rs879126000
NC_012920.1(MT-CYB):m.12171A>G rs1603223589
NC_012920.1(MT-CYB):m.12172A>G rs1556424073
NC_012920.1(MT-CYB):m.12173T>C rs1556424075
NC_012920.1(MT-CYB):m.12178C>T rs1603223596
NC_012920.1(MT-CYB):m.12188T>C rs879128211
NC_012920.1(MT-CYB):m.12189T>C rs28505538
NC_012920.1(MT-CYB):m.12191C>T rs1603223610
NC_012920.1(MT-CYB):m.12193A>G rs1603223611
Single allele rs376606918
m.12192G>A rs3134560

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.